Van Cott K E, Lubon H, Russell C G, Butler S P, Gwazdauskas F C, Knight J, Drohan W N, Velander W H
Department of Chemical Engineering, Virginia Tech, Blacksburg 24061, USA.
Transgenic Res. 1997 May;6(3):203-12. doi: 10.1023/a:1018442124584.
The genotypic and phenotypic stability of four lines of transgenic pigs expressing recombinant human protein C in milk was examined. Two lines were established with a construct consisting of a 2.6 kb mouse WAP promoter and a 9.4 kb human protein C genomic DNA. Two lines were established with another construct consisting of a 4.1 kb mouse WAP promoter and a 9.4 kb human protein C genomic DNA. Genotypic stability was measured by transgene copy number transmission. Outbred offspring having a single transgene integration locus were established from a founder having three independent, multicopy loci. Phenotypic stability over multiple lactations was defined by the combination of recombinant human protein C expression levels and the isoform signature of recombinant human protein C in western blots. Both cDNA and genomic human protein C transgenes gave similar ranges of expression levels of about 100-1800 micrograms ml-1. Within a given outbred lineage having a single loci for the cDNA transgene, the expression levels ranged between 100-400 micrograms ml-1. Western blots of reduced recombinant protein C revealed that single chain content was not dependent on expression level and was consistent within each transgenic line, but varied between transgenic lines. This suggests that native swine genetics may play a role in selection of production herds with optimal post-translational proteolytic processing capability. Although swine are not conventional dairy livestock, it is agreed that the short generation times, multiple offspring per litter, stable paternal transmission of the transgene, and milk production capabilities of swine offer distinct advantages over conventional dairy livestock for the establishment of a herd producing a therapeutic recombinant protein.
对四株在乳汁中表达重组人蛋白C的转基因猪品系的基因型和表型稳定性进行了检测。其中两株是用由2.6 kb小鼠WAP启动子和9.4 kb人蛋白C基因组DNA组成的构建体建立的。另外两株是用由4.1 kb小鼠WAP启动子和9.4 kb人蛋白C基因组DNA组成的另一种构建体建立的。通过转基因拷贝数传递来测定基因型稳定性。从具有三个独立多拷贝位点的奠基者中培育出具有单个转基因整合位点的远交后代。通过重组人蛋白C表达水平和蛋白质印迹中重组人蛋白C的异构体特征的组合来定义多个泌乳期的表型稳定性。cDNA和基因组人蛋白C转基因的表达水平范围相似,约为100 - 1800微克/毫升。在具有cDNA转基因单个位点的给定远交谱系中,表达水平在100 - 400微克/毫升之间。还原型重组蛋白C的蛋白质印迹显示,单链含量不依赖于表达水平,在每个转基因品系内是一致的,但在转基因品系之间有所不同。这表明本地猪的遗传学可能在选择具有最佳翻译后蛋白水解加工能力的生产猪群中发挥作用。虽然猪不是传统的奶牛家畜,但人们一致认为,猪的世代时间短、每窝产仔多、转基因的父系稳定传递以及产奶能力,与传统奶牛家畜相比,在建立生产治疗性重组蛋白的猪群方面具有明显优势。